蛋白质组学对近视发展的启示:蛋白质表达差异和钙信号在豚鼠形觉剥夺性近视中的作用

Rongbin Liang , Tao Li , Wenqing Shi , Hui Gao , Bei Ai , Bing Li , Xiaodong Zhou
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引用次数: 0

摘要

本研究旨在探讨豚鼠形觉剥夺性近视(FDM)玻璃体蛋白质组学的变化,从而揭示近视发生和发展的分子机制。通过用乳胶珠囊覆盖豚鼠的一只眼睛4周,成功建立了豚鼠近视模型。本研究利用四维数据独立采集蛋白质组学技术分析了FDM组和对照组的玻璃体样本。蛋白质组学分析的目的是确定 FDM 豚鼠玻璃体内蛋白质表达的差异。FDM 组在建模 4 周后成功诱导出近视。共鉴定出 6298 个蛋白质,其中 348 个为差异表达蛋白质(DEPs),81 个上调,267 个下调。对这些差异表达蛋白进行了深入的生物信息学分析,包括基因本体、真核同源组和京都基因和基因组百科全书。这些分析揭示了钙信号在细胞过程、代谢途径、生物调控、细胞骨架组织和细胞运动中的重要参与。我们的研究结果表明,钙信号在介导与形式剥夺相关的眼睛变化中起着关键作用,这可能与神经退行性疾病中观察到的机制相似。我们共发现了 348 个与近视的发生和发展相关的 DEPs。这些变化涉及关键的生物过程,包括蛋白质降解、细胞粘附和运输,尤其是钙信号通路的改变。基质相互作用分子 1(STIM1)是 FDM 的重要生物学标志物,这一点已通过 Western 印迹、免疫组织化学和 ELISA 得到证实。我们的研究发现,在近视豚鼠的发育过程中,玻璃体内蛋白质的表达存在明显差异,尤其是与钙信号通路相关的蛋白质。我们的研究为近视的发病机制,尤其是与蛋白质代谢途径相关的变化提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Proteomic insights into myopia development: Differential protein expression and the role of calcium signaling in form deprivation myopia in Guinea pigs

This study aims to explore the changes in the vitreous proteomics of form deprivation myopia (FDM) in guinea pigs, in order to reveal the molecular mechanisms involved in the onset and development of myopia. The myopia model in guinea pigs was successfully established by covering one eye of the guinea pigs with a latex bead sac for 4 weeks. This study used 4D data-independent acquisition proteomics technology to analyze vitreous body samples from both the FDM group and the control group. The goal of the proteomics analysis was to identify differences in protein expression within the vitreous body of FDM guinea pigs. Myopia was successfully induced in the FDM group after 4 weeks of modeling. A total of 6298 proteins were identified, among which 348 were differentially expressed proteins (DEPs), with 81 upregulated and 267 downregulated. These DEPs were subjected to in-depth bioinformatics analyses, including Gene Ontology, the Eukaryotic Orthologous Groups, and the Kyoto Encyclopedia of Genes and Genomes. These analyses revealed significant involvement in cellular processes, metabolic pathways, biological regulation, cytoskeletal organization, and cell movement. Our results indicate that calcium signaling plays a critical role in mediating eye changes associated with form deprivation, which may bear similarities to mechanisms observed in neurodegenerative diseases. A total of 348 DEPs related to the development and progression of myopia were identified. These changes involve key biological processes, including protein degradation, cell adhesion, and transport, especially alterations in calcium signaling pathways. Stromal interaction molecule 1 (STIM1) is an important biological marker of FDM, which was confirmed by Western blot, immunohistochemistry and ELISA. Our study found clear differences in the expression of proteins in the vitreous during the development of myopic guinea pigs, especially those related to calcium signaling pathway. Our study offers new insights into the pathogenesis of myopia, particularly changes related to protein metabolism pathways.

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